Mayo Clinic Center for Sleep Medicine, Mayo Clinic College of Medicine and Science, Rochester, MN, USA.
Department of Medicine (Division of Pulmonary, Critical Care, and Sleep Medicine), Rochester, MN, USA.
Neurotherapeutics. 2021 Jan;18(1):181-201. doi: 10.1007/s13311-021-01020-x. Epub 2021 Mar 30.
Associations between sleep disorders and neurological autoimmunity have been notably expanding recently. Potential immune-mediated etiopathogenesis has been proposed for various sleep disorders including narcolepsy, Kleine-Levin syndrome, and Morvan syndrome. Sleep manifestations are also common in various autoimmune neurological syndromes, but may be underestimated as overriding presenting (and potentially dangerous) neurological symptoms often require more urgent attention. Even so, sleep dysfunction has been described with various neural-specific antibody biomarkers, including IgLON5; leucine-rich, glioma-inactivated protein 1 (LGI1); contactin-associated protein 2 (CASPR2); N-methyl-D-aspartate (NMDA)-receptor; Ma2; dipeptidyl-peptidase-like protein-6 (DPPX); alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPA-R); anti-neuronal nuclear antibody type-1 (ANNA-1, i.e., Hu); anti-neuronal nuclear antibody type-2 (ANNA-2, i.e., Ri); gamma-aminobutyric acid (GABA)-B-receptor (GABA-B-R); metabotropic glutamate receptor 5 (mGluR5); and aquaporin-4 (AQP-4). Given potentially distinctive findings, it is possible that sleep testing could potentially provide objective biomarkers (polysomnography, quantitative muscle activity during REM sleep, cerebrospinal fluid hypocretin-1) to support an autoimmune diagnosis, monitor therapeutic response, or disease progression/relapse. However, more comprehensive characterization of sleep manifestations is needed to better understand the underlying sleep disruption with neurological autoimmunity.
睡眠障碍与神经自身免疫之间的关联最近显著扩大。包括嗜睡症、克莱恩-莱文综合征和莫尔万综合征在内的各种睡眠障碍,都提出了潜在的免疫介导的病因发病机制。各种自身免疫性神经综合征中也常见睡眠表现,但可能被低估,因为首要出现的(且可能危险的)神经症状往往需要更紧急的关注。即便如此,睡眠功能障碍也已经通过各种神经特异性抗体生物标志物描述过,包括 IgLON5;亮氨酸丰富的,神经胶质瘤失活蛋白 1(LGI1);接触蛋白相关蛋白 2(CASPR2);N-甲基-D-天冬氨酸(NMDA)-受体;Ma2;二肽基肽酶样蛋白 6(DPPX);α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPA-R);神经元核抗体 1 型(ANNA-1,即 Hu);神经元核抗体 2 型(ANNA-2,即 Ri);γ-氨基丁酸(GABA)-B 受体(GABA-B-R);代谢型谷氨酸受体 5(mGluR5);和水通道蛋白 4(AQP-4)。鉴于潜在的独特发现,睡眠测试可能提供客观的生物标志物(多导睡眠图、快速眼动睡眠期间的定量肌肉活动、脑脊液食欲素-1)来支持自身免疫诊断、监测治疗反应或疾病进展/复发,是有可能的。然而,需要更全面地描述睡眠表现,以更好地了解神经自身免疫中的潜在睡眠障碍。